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敏化引发的电子转移上转换:机理与光催化应用

Sensitization-initiated electron transfer upconversion: mechanism and photocatalytic applications.

作者信息

Glaser Felix, Kerzig Christoph, Wenger Oliver S

机构信息

Department of Chemistry, University of Basel St. Johanns-Ring 19 4056 Basel Switzerland

出版信息

Chem Sci. 2021 Jul 1;12(29):9922-9933. doi: 10.1039/d1sc02085d. eCollection 2021 Jul 28.

Abstract

Sensitization-initiated electron transfer (SenI-ET) describes a recently discovered photoredox strategy that relies on two consecutive light absorption events, triggering a sequence of energy and electron transfer steps. The cumulative energy input from two visible photons gives access to thermodynamically demanding reactions, which would be unattainable by single excitation with visible light. For this reason, SenI-ET has become a very useful strategy in synthetic photochemistry, but the mechanism has been difficult to clarify due to its complexity. We demonstrate that SenI-ET can operate sensitized triplet-triplet annihilation upconversion, and we provide the first direct spectroscopic evidence for the catalytically active species. In our system comprised of -[Ir(ppy)] as a light absorber, 2,7-di--butylpyrene as an annihilator, and ,-dimethylaniline as a sacrificial reductant, all photochemical reaction steps proceed with remarkable rates and efficiencies, and this system is furthermore suitable for photocatalytic aryl dehalogenations, pinacol couplings and detosylation reactions. The insights presented here are relevant for the further rational development of photoredox processes based on multi-photon excitation, and they could have important implications in the greater contexts of synthetic photochemistry and solar energy conversion.

摘要

敏化引发电子转移(SenI-ET)描述了一种最近发现的光氧化还原策略,该策略依赖于两个连续的光吸收事件,引发一系列能量和电子转移步骤。来自两个可见光子的累积能量输入使得能够进行热力学上要求苛刻的反应,而单靠可见光激发是无法实现这些反应的。因此,SenI-ET已成为合成光化学中一种非常有用的策略,但由于其复杂性,其机制一直难以阐明。我们证明SenI-ET可以实现敏化三重态-三重态湮灭上转换,并且我们为催化活性物种提供了首个直接光谱证据。在我们由作为光吸收剂的-[Ir(ppy)]、作为湮灭剂的2,7-二-丁基芘以及作为牺牲还原剂的,-二甲基苯胺组成的体系中,所有光化学反应步骤都以显著的速率和效率进行,并且该体系还适用于光催化芳基脱卤、频哪醇偶联和脱甲苯磺酰基反应。本文所展示的见解对于基于多光子激发的光氧化还原过程的进一步合理发展具有重要意义,并且它们可能在合成光化学和太阳能转换的更广泛背景中具有重要影响。

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